Canonical Allele Identifier: CA1328680977

Gene: PNKD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218270583A= , CM000664.2:g.218270583A=	GRCh38
NC_000002.11:g.219135306A= , CM000664.1:g.219135306A=	GRCh37
NC_000002.10:g.218843550A=	NCBI36
NG_017060.1:g.5192A=
NG_033036.1:g.4588T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436005.3:c.48A=	ENSP00000414400.3:p.Arg16=
ENST00000472650.2:n.73A=
ENST00000684905.1:n.59A=
ENST00000685415.1:c.48A=	ENSP00000510415.1:p.Arg16=
ENST00000687736.1:c.48A=	ENSP00000509627.1:p.Arg16=
ENST00000688179.1:c.48A=	ENSP00000508635.1:p.Arg16=
ENST00000689816.1:c.48A=	ENSP00000508450.1:p.Arg16=
ENST00000690891.1:c.48A=	ENSP00000509744.1:p.Arg16=
ENST00000691220.1:c.48A=	ENSP00000509580.1:p.Arg16=
ENST00000691799.1:n.71-798A=
ENST00000692260.1:n.63A=
ENST00000273077.9:c.48A= MANE Select	ENSP00000273077.4:p.Arg16=
ENST00000248451.7:c.48A=	ENSP00000248451.3:p.Arg16=
ENST00000273077.8:c.48A=	ENSP00000273077.4:p.Arg16=
ENST00000469689.1:n.64A=
NM_001077399.2:c.48A=	NP_001070867.1:p.Arg16=
NM_015488.4:c.48A=	NP_056303.3:p.Arg16=
XM_017003771.1:c.48A=	XP_016859260.1:p.Arg16=
NM_015488.5:c.48A= MANE Select	NP_056303.3:p.Arg16=
NM_001077399.3:c.48A=	NP_001070867.1:p.Arg16=